This service provides on-demand, specialized, efficient, and collaborative research support that is tailored to meet various research needs, including:
- Consultancy: conceptualizing research study, selecting and/or developing appropriate data collections processes and other research methodology. This is applicable to clinical trial, quality improvement initiatives and program evaluation-type of study.
- Regulatory compliance: reviewing and submitting regulatory documents to COMIRB/HSR/SARC/ORRQIRP, OnCore set up and regulatory sign-off.
- Study activities: setting up study binder, managing study participant reimbursement, designing and maintaining research databases (REDCap), designing and administering surveys (e.g., SurveyMonkey, Qualtrics, REDCap, etc.), recruiting and consenting study participants, monitoring study status, short-term personnel coverage, translating documents
Research Operations (Non-Clinical Trial): Jessica Holmes, PhD (as lead); Kasey Abrahamson, MPH, Sarah Nickles, BS, Shaelyn Solenske, BS, Emerald Saldyt, BS, Gabriella Peralta Reyes, BA, Tennyson Dahlman, BS, Eddy Panklang, BS, Lily Berkowitz, MPH (as research assistants)
Research Operations (Clinical Trial): Jessica Scott, MA, MPH (as lead); Lauren Turow, MA, Harmony Soffer, BA (as research assistants)